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Mutations of PHOX2B Gene in Patients of Obesity Hypoventilation Syndrome in Central India

Background Paired-like homeobox 2B (PHOX2B) gene on chromosome 4p12 codes for a transcription factor having a role in the formation of noradrenergic neuronal circuits. Its mutations have been linked to congenital central hypoventilation syndrome (CCHS). The clinical presentation of both, obesity hy...

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Detalles Bibliográficos
Autores principales:	Tyagi, Ankita, Goyal, Abhishek, Chaware, Prashant, Rathinam, Bertha A.D.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Thieme Medical and Scientific Publishers Pvt. Ltd. 2021
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381314/ https://www.ncbi.nlm.nih.gov/pubmed/35982870 http://dx.doi.org/10.1055/s-0041-1735582

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